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Imaging of organelles by electron microscopy reveals protein-protein interactions in mitochondria and chloroplasts
- Source :
- FEBS Letters. 584:2510-2515
- Publication Year :
- 2010
- Publisher :
- Wiley, 2010.
-
Abstract
- Ongoing progress in electron microscopy (EM) offers now an opening to visualize cells at the nanoscale by cryo-electron tomography (ET). Large protein complexes can be resolved at near-atomic resolution by single particle averaging. Some examples from mitochondria and chloroplasts illustrate the possibilities with an emphasis on the membrane organization. Cryo-ET performed on non-chemically fixed, unstained, ice-embedded material can visualize specific large membrane protein complexes. In combination with averaging methods, 3D structures were calculated of mitochondrial ATP synthase at 6nm resolution and of chloroplast photosystem II at 3.5nm.
- Subjects :
- Electron Microscope Tomography
Supercomplex
Chloroplasts
SINGLE-PARTICLE RECONSTRUCTION
Photosystem II
Single particle electron microscopy
CRYOELECTRON TOMOGRAPHY
CRYOMICROSCOPY
Biophysics
ORGANIZATION
Biology
Mitochondrion
Chloroplast
Biochemistry
Protein–protein interaction
law.invention
Mitochondrial Proteins
Structural Biology
law
Organelle
Electron microscopy
ATOMIC-RESOLUTION
Genetics
Nanotechnology
Protein Interaction Domains and Motifs
Tomography
Molecular Biology
Organelles
ARCHITECTURE
ATP SYNTHASE
ATP synthase
Cryoelectron Microscopy
Resolution (electron density)
Membrane Proteins
Photosystem II Protein Complex
food and beverages
Cell Biology
Mitochondria
Cell biology
Microscopy, Electron
Multiprotein Complexes
biology.protein
COMPLEXES
MEMBRANE
Electron microscope
Subjects
Details
- ISSN :
- 00145793
- Volume :
- 584
- Database :
- OpenAIRE
- Journal :
- FEBS Letters
- Accession number :
- edsair.doi.dedup.....1ca4e4c969a29fe8b70792b77cb57f2e